HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 21110474, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Furan-3,4-diyldimethanol | HCID 84477 | — |
| Reactant | HCID 21110455 | HCID 21110455 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21110474 | HCID 21110474 | — |
Reaction Steps
According to a similar procedure to that described in Example 21-(2), 3,4-furandimethanol (described in J. Org. Chem., 65, 6153 (2000); 3.4 g, 26.5 mmol) was reacted with imidazole (1.80 g, 26.4 mmol) and tert-butylchlorodimethylsilane (4.00 g, 26.5 mmol) in tetrahydrofuran (50 ml), and the reaction mixture was worked up to afford a mixture of the title compound, 3,4-furandimethanol and 3,4-bis[(tert-butyldimethylsilyl)oxymethyl]furan. The mixture was subjected to chromatography on a silica gel (50 g) column (eluent; ethyl acetate:hexane=3:17˜4:16) to afford the title compound (3.20 g, 50% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230023B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-92d40dcfcfc94649a5f48ee40d2e73bf |
| Source note | uspto-grants-2007_06 |